Canonical Allele Identifier: CA2455035139
Gene: GLUD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.121048405G= , CM000685.2:g.121048405G= GRCh38
NC_000023.10:g.120182259G= , CM000685.1:g.120182259G= GRCh37
NC_000023.9:g.120009940G= NCBI36
NG_016456.1:g.5798G=

Transcript Alleles

HGVS Amino-acid change
ENST00000328078.3:c.721G= MANE Select ENSP00000327589.1:p.Ala241=
ENST00000328078.2:c.721G= ENSP00000327589.1:p.Ala241=
NM_012084.3:c.721G= NP_036216.2:p.Ala241=
NM_012084.4:c.721G= MANE Select NP_036216.2:p.Ala241=